HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1170768Generated: November 2, 2026
Sodium borohydride → 1-(4-(3-Bromopropyl)phenyl)ethanol
https://huagongshe.com/reaction/1170768
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 1-(4-Acetylphenyl)-3-bromopropane | HCID 14817035 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-(4-(3-Bromopropyl)phenyl)ethanol | HCID 67523991 | — |
Reaction Steps
Also disclosed herein is a method of making 4-vinylbenzenepropanethiol. The method includes providing 1-bromo-3-phenylpropane, adding acetic anhydride and aluminum chloride, incubating the mixture at from about −20 to about 20 degrees Celsius for from about 1 hour to about 12 hours, isolating the resulting p-(3-bromopropyl)acetophenone, adding sodium borohydride to the p-(3-bromopropyl)acetophenone solution in methanol, incubating the mixture at about 0 degrees Celsius for about 2 hours, isolating the resulting p-(3-bromopropyl)-α-methylbenzenemethanol, adding toluensulfonic acid to the solution of p-(3-bromopropyl)-α-methylbenzenemethanol in toluene, refluxing the mixture under inert atmosphere for about 4 hours, isolating the resulting p-(3-Bromopropyl)styrene, adding thiourea to the p-(3-Bromopropyl)styrene, gently refluxing the mixture for about 16 hours, adding sodium hydroxide, and gently refluxing the mixture for about 4 hours.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07829155B1 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-1107a1ba0ee2402cbeeb9d3848505015 |
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| Source note | uspto-grants-2010_11 |
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